Suppr超能文献

在伤害性三叉神经血管激活的动物模型中比较传统的中西方偏头痛药物的效果。

Comparative effects of traditional Chinese and Western migraine medicines in an animal model of nociceptive trigeminovascular activation.

机构信息

1 Department of Neurology, University of California, San Francisco, CA, USA.

2 Basic and Clinical Neurosciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

出版信息

Cephalalgia. 2018 Jun;38(7):1215-1224. doi: 10.1177/0333102417728245. Epub 2017 Aug 24.

Abstract

Background Migraine is a highly prevalent and disabling disorder of the brain with limited therapeutic options, particularly for preventive treatment. There is a need to identify novel targets and test their potential efficacy in relevant preclinical migraine models. Traditional Chinese medicines have been used for millennia and may offer avenues for exploration. Methods We evaluated two traditional Chinese medicines, gastrodin and ligustrazine, and compared them to two Western approaches with propranolol and levetiracetam, one effective and one ineffective, in an established in vivo rodent model of nociceptive durovascular trigeminal activation. Results Intravenous gastrodin (30 and 100 mg/kg) significantly inhibited nociceptive dural-evoked neuronal firing in the trigeminocervical complex. Ligustrazine (10 mg/kg) and propranolol (3 mg/kg) also significantly inhibited dural-evoked trigeminocervical complex responses, although the timing of responses of ligustrazine does not match its pharmacokinetic profile. Levetiracetam had no effects on trigeminovascular responses. Conclusion Our data suggest gastrodin has potential as an anti-migraine treatment, whereas ligustrazine seems less promising. Interestingly, in line with clinical trial data, propranolol was effective and levetiracetam not. Exploration of the mechanisms and modelling effects of Chinese traditional therapies offers novel route for drug discovery in migraine.

摘要

背景

偏头痛是一种高发且致残性的脑部疾病,治疗选择有限,尤其是预防性治疗。因此,需要确定新的靶点,并在相关的偏头痛临床前模型中测试其潜在疗效。传统中药已经使用了数千年,可能为探索提供了途径。

方法

我们评估了两种传统中药,天麻素和川芎嗪,并将其与两种西药,普萘洛尔和左乙拉西坦进行比较,这两种西药中一种有效,一种无效,在一种已建立的伤害性硬脑膜血管三叉神经激活的体内啮齿动物模型中进行比较。

结果

静脉注射天麻素(30 和 100mg/kg)可显著抑制三叉神经颈复合体中伤害性硬脑膜诱发的神经元放电。川芎嗪(10mg/kg)和普萘洛尔(3mg/kg)也显著抑制硬脑膜诱发的三叉神经颈复合体反应,尽管川芎嗪的反应时间与其药代动力学特征不匹配。左乙拉西坦对三叉血管反应没有影响。

结论

我们的数据表明天麻素具有作为偏头痛治疗药物的潜力,而川芎嗪则不太可能。有趣的是,与临床试验数据一致,普萘洛尔有效,而左乙拉西坦无效。探索中药的作用机制和模型效应为偏头痛的药物发现提供了新的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/119a/6024356/3f9d45eccc6b/10.1177_0333102417728245-fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验